Abstract |
Dyschromatosis universalis hereditaria (DUH) is a rare autosomal dominant inherited dermatosis which usually appears during childhood and is characterized by dyspigmentation, with both hypopigmented and hyperpigmented macules. We report a case of DUH with unexplained childhood-onset renal failure. The association between DUH and renal failure is yet to be proven by further studies.
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Authors | Salinee Rojhirunsakool, Vasanop Vachiramon |
Journal | Case reports in dermatology
(Case Rep Dermatol)
Vol. 7
Issue 1
Pg. 51-5
( 2015)
ISSN: 1662-6567 [Print] Switzerland |
PMID | 25969678
(Publication Type: Case Reports)
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